Canonical Allele Identifier: CA886010333

Gene: PTGFRN

Linked Data

• dbSNP Id: rs1350692690
• MyVariant Identifiers: chr1:g.117467886T>A (hg19) ; chr1:g.116925264T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116925264T>A , CM000663.2:g.116925264T>A	GRCh38
NC_000001.10:g.117467886T>A , CM000663.1:g.117467886T>A	GRCh37
NC_000001.9:g.117269409T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393203.3:c.49+15012T>A MANE Select	ENSP00000376899.2:n.49+15012T>A
ENST00000393203.2:c.49+15012T>A	ENSP00000376899.2:n.49+15012T>A
NM_020440.3:c.49+15012T>A	NP_065173.2:n.49+15012T>A
NM_020440.4:c.49+15012T>A MANE Select	NP_065173.2:n.49+15012T>A